ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.11586C>T (p.Cys3862=)

dbSNP: rs2130975528
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002082267 SCV002421437 likely benign Cohen syndrome 2021-11-26 criteria provided, single submitter clinical testing

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